-
We have published a statement by the UK CF Medical Association with advice to people with
#cysticfibrosis and their families on the#coronavirus outbreak:https://www.cysticfibrosis.org.uk/the-work-we-do/about-us/statements … -
Osobe Vidi sve
Ovjeren akaunt@CF_Foundation The Cystic Fibrosis Foundation is the world’s leader in the search for a cure for cystic fibrosis.
-
What cystic fibrosis symptoms can I learn to self-manage?
#CF#CysticFibrosis https://raremark.com/cystic-fibrosis/articles/what-cystic-fibrosis-symptoms-can-i-learn-to-self-manage--1148 …pic.twitter.com/EyHmh9xetU
-
Supporting employees, charities and the community... Brownlow are proud to be part of the
#jordanwhitehouse memorial tournament to be held 6th June 2020#7aside#football#cysticfibrosis. Want to be involved? Have a raffle prize? Pls contact ianwhitehouse21@gmail.com pic.twitter.com/lb9Qqr7QuE
-
Listen to the latest podcast from
@GorbalsSTEM where Dr Maria Jackson speaks to Summer about the Genetics of#cysticfibrosis@Diane__Murray#CFhttps://twitter.com/GorbalsSTEM/status/1225011184618749957 …
0:43 -
a previous job told me “it’s best if no one finds out you have
#cysticfibrosis employment will be terminated” when asking for annual leave for a hosp app same people cancelled someone’s interview once he’d declared he was in a wheelchair. They’ve since gone into administration
https://twitter.com/dwp/status/1224281564575621121 … -
Know the feeling of being told you won't live long.
#CysticFibrosis and hit 30 boo yaa 50 next. I love his drive! Follow him if you haven't. https://twitter.com/realyungcripp/status/1224961587221618689 … -
.
@AnnaMKaplan: your constituents with#cysticfibrosis need your support. Please protect the Adult Cystic Fibrosis Assistance Program from being eliminated in the 2021 budget. Adults with CF rely on this program to access their care and treatments#CFadvocacy -
Conor burns in his Mascot outfit for the
#CysticFibrosis Sunday 9th feb at Seaview pic.twitter.com/XR8vl2SM4M
-
Can anyone with
#CysticFibrosis DM me?
-
It’s fucking heartbreaking seeing certain people with
#CysticFibrosis at end stage pleading for access to#Trikafta. It should be a no brainer. But what’s even more heartbreaking is the fact that access shouldn’t be granted at this stage. It’s almost too late & the damage is donePrikaži ovu nit -
ITS HERE! First dose officially taken! So excited
#Symkevi#cysticfibrosis pic.twitter.com/XewBJ5Z2eo
Prikaži ovu nit -
Scientists have combined doses of three antibiotics -- amoxicillin & imipenem-relebactam & found it was 100% effective in killing off the infection which is usually extremely difficult to treat in patients with cystic fibrosis.
#cysticfibrosis. pic.twitter.com/iaZAqBHjPW
Prikaži ovu nit -
Wishing everyone in the
#cysticfibrosis community a great week ahead! -
-
2nd lot of IV antibiotics for number 2 son this year and it’s only February! I wish life would give him a break.
#cysticfibrosis
pic.twitter.com/pkAn1Ci0ee
-
Welcome to February Beamers! Here is this week's live class lineup! We're always here to support you in your goals and ways you can stay active in your lives.
https://beamfeelgood.com/onDemand/liveClasses/cystic-fibrosis …
#beamfeelgood#cysticfibrosis#movementtofeelgoodpic.twitter.com/Xh8GQUUupA
-
We oppose new CMS guidance allowing state
#Medicaid programs to apply for block grants or per capita caps and will educate stakeholders on how this will reduce access to quality, affordable care for people with#preex, like#cysticfibrosis.#DefendPreEx#CFAdvocacyhttps://twitter.com/LungAssociation/status/1222905277357481984 … -
We stand with UKCFMA in urging
@MattHancock to do everything he can to make the triple therapy available.#cysticfibrosis https://bit.ly/36EgIez pic.twitter.com/Y1XtPCJoqU
-
After 9 weeks, almost dying, being in a coma for 12 days I’m going home!!!!!!!!!!
#secondchanceatlife#cysticfibrosis#kidneyfailure#organdonation#icupic.twitter.com/4HRdmNhZPV
-
A bacterial lung infection has lingered in Gracie's lungs since she was 3 months old. After a recent stay at our hospital, her parents are hopeful that the infection is behind them now. Her parents say she's their "little
#cysticfibrosis fighter", and we think that's fitting!
pic.twitter.com/0knr2R3mFw
Čini se da učitavanje traje već neko vrijeme.
Twitter je možda preopterećen ili ima kratkotrajnih poteškoća u radu. Pokušajte ponovno ili potražite dodatne informacije u odjeljku Status Twittera.